HOBSCOTCH Phase III

Sponsor
Dartmouth-Hitchcock Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT04519775
Collaborator
Centers for Disease Control and Prevention (U.S. Fed)
116
1
2
45.6
2.5

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the efficacy of an entirely virtual version of the home-based cognitive self-management program "HOBSCOTCH." It will test whether HOBSCOTCH can be delivered nationally from a distance utilizing e-health tools (telephone, computer, and phone).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Home Based Self-management and Cognitive Training Changes lives (HOBSCOTCH)
N/A

Detailed Description

HOBSCOTCH (Home Based Self-management and Cognitive Training Changes lives) is a home-based self-management program to treat cognitive symptoms and improve quality of life, while minimizing the barriers of access to care. The program is based on Problem Solving Therapy (PST) and teaches problem solving strategies and compensatory mechanisms to help manage cognitive dysfunction and enhance quality of life.

HOBSCOTCH Phase III is a study to examine an entirely virtual version of the program. While HOBSCOTCH was shown to be effective as an in-person and telephone-based program in previous trials (HOBSCOTCH Phase I and II), this study aims to test a version of the program adapted for entirely virtual delivery. This is a single-center study, with the HOBSCOTCH intervention being delivered by staff affiliated with Dartmouth-Hitchcock Medical Center in Lebanon, NH.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
116 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
HOBSCOTCH Phase III: Efficacy of Enhanced Virtual HOBSCOTCH
Actual Study Start Date :
Nov 12, 2020
Anticipated Primary Completion Date :
Sep 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: HOBSCOTCH-V (virtual)

Participants will receive the HOBSCOTCH intervention consisting of 1:1 sessions delivered once per week, including: 1 pre-HOBSCOTCH Session (on webcam) 1 educational session (on webcam) 6 telephone sessions 1 wrap-up session (webcam or telephone) Participants will also receive 3 booster sessions, via webcam or telephone, once per month.

Behavioral: Home Based Self-management and Cognitive Training Changes lives (HOBSCOTCH)
HOBSCOTCH is a home-based self-management program to treat cognitive symptoms and improve quality of life, while minimizing the barriers of access to care. The program is based on Problem Solving Therapy (PST) and teaches problem solving strategies and compensatory mechanisms to help manage cognitive dysfunction and enhance quality of life.
Other Names:
  • HOBSCOTCH
  • Other: Control

    Participants will be wait listed and will receive HOBSCOTCH-V (above) following a 6 month wait period.

    Behavioral: Home Based Self-management and Cognitive Training Changes lives (HOBSCOTCH)
    HOBSCOTCH is a home-based self-management program to treat cognitive symptoms and improve quality of life, while minimizing the barriers of access to care. The program is based on Problem Solving Therapy (PST) and teaches problem solving strategies and compensatory mechanisms to help manage cognitive dysfunction and enhance quality of life.
    Other Names:
  • HOBSCOTCH
  • Outcome Measures

    Primary Outcome Measures

    1. Change in quality of life [Baseline and at months 3, 6, 9, 12]

      The researchers will use the Quality of Life in Epilepsy (QOLIE-31). This validated tool contains 16 multi-item scales which assess health related quality of life, emotional well-being, memory and attention deficits, medication effects, seizure control, psychosocial functioning, and health perception. Scores range from 0 to 100, with a higher score reflecting a higher quality of life.

    2. Change in cognitive function [Baseline and at months 3, 6, 9, 12]

      The researchers will use the Cognitive Function sub-scale of the NeuroQOL. This is a brief validated tool developed by the NIH for use in patients with neurological disease. Scores range from 8 to 40, with a higher score indicating better reported cognitive functioning.

    Secondary Outcome Measures

    1. Change in depression [Baseline and at months 3, 6, 9, 12]

      The researchers will use the Patient Health Questionnaire (PHQ-9). The PHQ-9 is a brief 9-item validated depression scale. Scores range from 0 to 27. Scores of 5, 10, 15, and 20 represent cut-offs for mild, moderate, moderately severe, and severe depression, respectively.

    2. Change in self-management practices [Baseline and at months 3, 6, 9, 12]

      The researchers will use the Adult Epilepsy Self-Management Measurement Instrument (AESMMI-65).This is a 65 item scale that assesses use of epilepsy self-management practices. Scores range from 65 to 325, with a higher score indicating more frequent use of self-management strategies.

    3. Changes in self-reported seizure frequency [Ongoing through entire study baseline - 12 months]

      The researchers will collect seizure information throughout the entire study by use of a smartphone app or paper log to track seizures daily. No range.

    4. Changes in medication adherence [Ongoing through entire study baseline - 12 months, and at baseline and at months 3, 6, 9, 12]

      Medication adherence will be collected using the Medication Adherence Rating Scale (MARS), a 10-item inventory to measure medication adherence, as well as by a daily single item medication adherence question through a smartphone app or paper log. For the MARS, scores range from 0 to 10, with a higher score indicating better adherence.

    5. Changes in health confidence [Baseline and at months 3, 6, 9, 12]

      The researchers will use the Health Confidence Score, a 4-item measure of health confidence. Scores range from 0 to 13, with a higher score indicating better health confidence.

    6. Changes in healthcare utilization [Baseline and at months 3, 6, 9, 12]

      The researchers will use the Health Care Utilization 4-item measure from the Self-Management Resource Center to capture utilization of health services in the last 6 months. No range.

    7. Changes in overall well-being [Ongoing through entire study baseline - 12 months]

      The researchers will collect daily well-being information throughout the entire study by use of a smartphone app or paper log and a basic single item Likert-scale of well-being. No range.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age 18+

    • Diagnosis of epilepsy, with controlled or uncontrolled seizures

    • Subjective memory complaints

    • No changes in antiepileptic and antidepressant medication regimen for 1 month, however brief discontinuation of antiepileptic medicine for inpatient video EEG evaluation is acceptable

    • Literate

    • Telephone access

    • Internet access

    Exclusion Criteria:
    • Subjects self-reporting a dementing illness or a mention of a dementing illness in their medical record

    • Severe mental disability or estimated IQ less than 70 per clinical judgement

    • Significant visual impairment precluding reading or writing

    • No reliable telephone or internet access

    • No diagnosis of epilepsy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dartmouth-Hitchcock Medical Center Lebanon New Hampshire United States 03756

    Sponsors and Collaborators

    • Dartmouth-Hitchcock Medical Center
    • Centers for Disease Control and Prevention

    Investigators

    • Principal Investigator: Barbara Jobst, MD, Dartmouth-Hitchcock Medical Center and Dartmouth College

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Barbara Jobst, Staff Physician, Neurology, Dartmouth-Hitchcock Medical Center
    ClinicalTrials.gov Identifier:
    NCT04519775
    Other Study ID Numbers:
    • D12217 Phase III
    First Posted:
    Aug 20, 2020
    Last Update Posted:
    Nov 22, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Barbara Jobst, Staff Physician, Neurology, Dartmouth-Hitchcock Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 22, 2021